through participation in client site visits, industry events, and other relevant activities. Drive the completion through participation in client site visits, industry events, and other relevant activities. Keep abreast with
all received product quality complaints, adverse events and medical enquiries to the relevant person in
all received product quality complaints, adverse events and medical enquiries to the relevant person in
virology related products. Is responsible for adverse event reporting and management of drug safety and pharmacovigilance
virology related products. Is responsible for adverse event reporting and management of drug safety and pharmacovigilance
medicine distributed are batch traceable in the event of a recall and that all invoices carry batch numbers
on Risk Assessments, CAPA, Change Controls, and Events to ensure timely closure and effectiveness of corrective
medicine distributed are batch traceable in the event of a recall and that all invoices carry batch numbers
on Risk Assessments, CAPA, Change Controls, and Events to ensure timely closure and effectiveness of corrective